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Gilberto J. Soler-Llavina

Researcher at Allen Institute for Brain Science

Publications -  21
Citations -  1872

Gilberto J. Soler-Llavina is an academic researcher from Allen Institute for Brain Science. The author has contributed to research in topics: AMPA receptor & Postsynaptic potential. The author has an hindex of 16, co-authored 20 publications receiving 1442 citations. Previous affiliations of Gilberto J. Soler-Llavina include Harvard University & Howard Hughes Medical Institute.

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Classification of electrophysiological and morphological neuron types in the mouse visual cortex.

TL;DR: A single-cell characterization pipeline is established using standardized patch-clamp recordings in brain slices and biocytin-based neuronal reconstructions to establish a morpho-electrical taxonomy of cell types for the mouse visual cortex via unsupervised clustering analysis of multiple quantitative features.
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B-Lymphocyte-Mediated Delayed Cognitive Impairment following Stroke

TL;DR: It is discovered that in mouse models, activated B-lymphocytes infiltrate infarcted tissue in the weeks after stroke and immunostaining of human postmortem tissue revealed that a B-LYmphocyte response to stroke also occurs in the brain of some people with stroke and dementia.
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Preparation of Acute Brain Slices Using an Optimized N-Methyl-D-glucamine Protective Recovery Method.

TL;DR: A substantial improvement is observed in the speed and reliability of gigaohm seal formation during targeted patch clamp recording experiments while maintaining excellent neuronal preservation, thereby facilitating challenging experimental applications.
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Synapse-specific plasticity and compartmentalized signaling in cerebellar stellate cells

TL;DR: Stellate cell dendrites spatially restrict signaling cascades that lead from CP-AMPAR activation to endocannabinoid production and trigger the selective regulation of active synapses, demonstrating input-specific synaptic plasticity.
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The neurexin ligands, neuroligins and leucine-rich repeat transmembrane proteins, perform convergent and divergent synaptic functions in vivo

TL;DR: Results show that neurexin ligands in vivo form a dynamic synaptic cell adhesion network, with compensation between NLs and LRRTMs during early synapse development and functional divergence upon synapse maturation.